"67046-525-07" National Drug Code (NDC)

NDC Code	67046-525-07
Package Description	7 TABLET, FILM COATED in 1 BLISTER PACK (67046-525-07)
Product NDC	67046-525
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Olanzapine
Non-Proprietary Name	Olanzapine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20171004
Marketing Category Name	ANDA
Application Number	ANDA202862
Manufacturer	Contract Pharmacy Services-PA
Substance Name	OLANZAPINE
Strength	10
Strength Unit	mg/1
Pharmacy Classes	Atypical Antipsychotic [EPC]